LiverQuant:肝脏病理定量分析的改进方法。

Dominick J Hellen, Saul J Karpen
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摘要

目前对肝脏组织切片的细胞、基因表达和纤维化进行量化的方法在研究界还没有标准化,通常依赖于从每张切片中随机选择的区域获取数据。因此,分析会受到选择偏差以及整个切片中可用数据元素子集有限的影响。对细胞和纤维化的整张切片分析将提供更准确、更完整的定量分析,并最大限度地减少实验内和实验间的变量。在此,我们介绍 LiverQuant,这是一种对数字化组织学图像进行全玻片扫描量化的方法,可对呈现的数据元素进行更全面的分析。在 QuPath 程序中加载图像并准备项目后,研究人员每次分析都能获得一到两个脚本,这些脚本能生成染色的平均强度阈值、自动组织注释以及预期细胞矩阵的下游检测。与组织学量化的两种标准方法相比,LiverQuant 有两个显著优势:速度更快,组织覆盖面积扩大了 50 倍。LiverQuant 使用公开的开源代码(GitHub),提高了实验结果的可靠性和可重复性,同时缩短了科学家对肝脏组织学进行批量分析所需的时间。大多数实验室都可以采用这种分析流程,只需进行最低限度的优化,而且其原理和代码经过优化后还可用于其他器官。图形概览。
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LiverQuant: An Improved Method for Quantitative Analysis of Liver Pathology.

Current means to quantify cells, gene expression, and fibrosis of liver histological slides are not standardized in the research community and typically rely upon data acquired from a selection of random regions identified in each slide. As such, analyses are subject to selection bias as well as limited subsets of available data elements throughout the slide. A whole-slide analysis of cells and fibrosis would provide for a more accurate and complete quantitative analysis, along with minimization of intra- and inter-experimental variables. Herein, we present LiverQuant, a method for quantifying whole-slide scans of digitized histologic images to render a more comprehensive analysis of presented data elements. After loading images and preparing the project in the QuPath program, researchers are provided with one to two scripts per analysis that generate an average intensity threshold for their staining, automated tissue annotation, and downstream detection of their anticipated cellular matrices. When compared with two standard methodologies for histological quantification, LiverQuant had two significant advantages: increased speed and a 50-fold greater tissue area coverage. Using publicly available open-source code (GitHub), LiverQuant improves the reliability and reproducibility of experimental results while reducing the time scientists require to perform bulk analysis of liver histology. This analytical process is readily adaptable by most laboratories, requires minimal optimization, and its principles and code can be optimized for use in other organs. Graphical overview.

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